Cas 710351-69-2,N-methyl-4-({1-methyl-2-[(4-methyl-3-pyrrolidin-1-ylphenyl)-amino]-1H-benzimidazol-5-yl}oxy)pyridine-2-carboxamide

710351-69-2

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Basic information

Product Name: N-methyl-4-({1-methyl-2-[(4-methyl-3-pyrrolidin-1-ylphenyl)-amino]-1H-benzimidazol-5-yl}oxy)pyridine-2-carboxamide
Synonyms: N-methyl-4-({1-methyl-2-[(4-methyl-3-pyrrolidin-1-ylphenyl)-amino]-1H-benzimidazol-5-yl}oxy)pyridine-2-carboxamide
CAS NO:710351-69-2
Molecular Formula:
Molecular Weight: 456.547
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-methyl-4-({1-methyl-2-[(4-methyl-3-pyrrolidin-1-ylphenyl)-amino]-1H-benzimidazol-5-yl}oxy)pyridine-2-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-methyl-4-({1-methyl-2-[(4-methyl-3-pyrrolidin-1-ylphenyl)-amino]-1H-benzimidazol-5-yl}oxy)pyridine-2-carboxamide(710351-69-2)
EPA Substance Registry System: N-methyl-4-({1-methyl-2-[(4-methyl-3-pyrrolidin-1-ylphenyl)-amino]-1H-benzimidazol-5-yl}oxy)pyridine-2-carboxamide(710351-69-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 710351-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 710351-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,0,3,5 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 710351-69:
(8*7)+(7*1)+(6*0)+(5*3)+(4*5)+(3*1)+(2*6)+(1*9)=122
122 % 10 = 2
So 710351-69-2 is a valid CAS Registry Number.

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710351-69-2Relevant academic research and scientific papers

Substituted benzazoles and methods of their use as inhibitors of Raf kinase

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Page 385, (2008/06/13)

New substituted benz-azole compounds, compositions and methods of inhibition of Raf kinase activity in a human or animal subject are provided. The new compounds compositions may be used either alone or in combination with at least one additional agent for the treatment of a Raf kinase mediated disorder, such as cancer.

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